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 Day 1 May 17, Thursday

8:30-9:00 Registration & Refresh Coffee

9:00-9:10 Welcome Remark

9:10-9:50 Mr. James J. HO, MD, PhD, DABCC,Professor, Director of Peking Union Medical College & Chinese Academy of Medical Sciences, Center for Clinical Laboratory Development; Chairman and CEO of Beijing Lawke Health Laboratory Co. Ltd.

Topic: Who Sets the Rules -- Chinese CRO Central Lab Going International

9:50-10:30 Mr. Charlie XU, MD, PhD, VP of Clinical Services at Frontage Lab China

Topic: Clinical CROs in China -- Prospective and Globalization

10:30-10:50 Coffee Break + Exhibition Visit

10:50-11:25 Mr. Zhenping WU, PhD, M.B.A. Senior Vice President, Pharmaceutical Sciences at HMP

Topic: Selection Criteria for Contract Organizations -- An Insider's View

11:25-12:00 Ms. Lin HE, PhD, Senior Director of Strategic Development Department of Shanghai Pharmaceutical Clinical Research Center

Topic: China and Global CRO Industrial Development Trends

12:00-13:30 Luncheon

13:30-14:10 Mr. Dan ZHANG, Chairman & CEO of Fountain Medical Development Ltd.

Topic: Managing Safety Issues in Clinical Development in China: The Role of CRO

14:10-14:50 Mr. Tony SONG, Manager of Life Science Market in 3M Purification division

Topic: Filtration Technologies in Pharmaceutical R&D Phase and 3M Validation Service

14:50-15:00 Q & A – All conference participants self-introduction

15:00-15:20 3M Release of Certification Laboratory

15:20-15:40 Coffee Break + Exhibition Visit

15:40-16:20 Ms. Weijun SHA, BD Director & Project Director of TigerMed

Topic: Creating New Valuable Working Model through Strategic Partnership with Clients

16:20-17:00 Panel Discussion – Q & A

 

Day2 May 18, Friday

9:00-9:40 Mr. Zhuohan HU, PhD, President & CEO, Research Institute for Liver Diseases (Shanghai) Inc.; Professor, Fudan University & Shanghai University of Chinese Medicines Shanghai, China

Topic: Bridging Discovery to Development in Therapeutic Innovation: Challenges and Solutions

9:40-10:20 Mr. James S. YAN, M.D. PhD, DABT, Senior Director and Site Scientific Lead of Covance Pharmaceutical R&D (Shanghai) Co., Ltd.

Topic: Project Management during Pharmaceutical Preclinical R&D: Study Design, Facilities and Data Interpretation

10:20-10:40 Coffee Break + Exhibition Visit

10:40-11:20 Mr. Yi YANG, PhD, RVT, Director of Preclinical Safety, DPE in Preclinical Safety of DSAR Asia-Pacific Sanofi-aventis China

Topic: Special Considerations in Preclinical Safety Assessment to Support Biopharmaceutical Development

11:20-12:00 Mr. Dylan Dalin YAO, MD, PhD, Senior VP & Chief Scientific Officer of Joinn Laboratories Inc.

Topic: Dual Solutions for Filing Nonclinical Pharm/Tox Data in Regulatory Submissions to Both the Domestic and International Agencies

12:00-13:30 Luncheon

13:30-14:10 Ms. Wen CAO, M.D, PhD, Manager of Phase I Clinical Trail in VPS Clinical Group.

Topic: Early Clinical Research on Drug Innovation

14:10-14:50 Mr. Ming GUO, PhD, Co-Founder & COO of Ascentage Pharma; General Manager of Small Molecule Drug R&D Center, China Medical City

Topic: An Experienced Partner in Late Discovery and IND Enabling at China Medical City

14:50-15:10 Coffee Break + Exhibition Visit

15:10-15:50 Mr. Zhenyu XUAN, PhD,General Manager of Suzhou Youseen New Drug R&D Co. Ltd., Senior Engineer; Professor of Shanghai University of TCM; Shanghai excellent academic leader

Topic: CRO Service for Traditional Chinese Medicine Development and the Entrance of TCM into Global Market

15:50-16:30 Panel Discussion – Q&A – Conference Conclusion

Package Plan

Before 29/2/2012: USD 440

After 29/2/2012: USD 540

 

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Chinese companies and academics reaching out to the western scientific community through attending meetings, publishing in scientific journals, etc is very important to address this problem. By not publishing more it is not only hurting China's growth but global growth as the opportunity to collaborate on research and find out about new discoveries is limited.

——Seth Goldenberg, President of Asia Pacific Bio Intelligence LLC

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